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Last Updated: 01/20/2023

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Found 5 publications

A Familial Form of Epidermolysis Bullosa Simplex Associated with a Pathogenic Variant in KRT5.

Journal: Genes
Published: October 23, 2021

Genetic and acquired blistering disorders of pediatric age group: An experience from Eastern India.

Journal: Indian journal of pathology & microbiology
Published: August 03, 2021

Gastrostomy for infants with severe epidermolysis bullosa simplex in neonatal intensive care.

Journal: Orphanet journal of rare diseases
Published: June 12, 2021

Basal pharmacokinetic parameters of topically applied diacerein in pediatric patients with generalized severe epidermolysis bullosa simplex.

Condition: Epidermolysis bullosa simplex
Journal: Orphanet journal of rare diseases
Treatment Used: Topically applied diacerein
Number of Patients: 0
Published: November 02, 2018

Diacerein orphan drug development for epidermolysis bullosa simplex: A phase 2/3 randomized, placebo-controlled, double-blind clinical trial.

Condition: Epidermolysis bullosa simplex (EBS)
Journal: Journal of the American Academy of Dermatology
Treatment Used: 1% diacerein cream
Number of Patients: 17
Published: February 08, 2018
Showing 1-5 of 5

Last Updated: 01/20/2023